Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43974830-43975046 | Common:3; Rare:63 | ||||
chr1:44674421-44674733 | Common:3; Rare:79 | ||||
chr1:44775480-44775610 | Rare:51 | ||||
chr1:44777611-44778117 | Common:2; Rare:126 | ||||
chr1:44986512-44986819 | Common:2; Rare:63; Clinvar (benign):1 | ||||
chr1:45012119-45012278 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339959-45340046 | Rare:30 | ||||
chr1:45340103-45340212 | Rare:50; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45340386-45340470 | Common:1; Rare:22; Clinvar:1 | ||||
chr1:45499987-45500341 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521833-45522087 | Common:1; Rare:100 | ||||
chr1:45550721-45551083 | Common:3; Rare:90 | ||||
chr1:45583931-45584077 | Rare:56 | ||||
chr1:45687059-45687318 | Common:1; Rare:70 | ||||
chr1:45688055-45688253 | Common:1; Rare:56 |